Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:28885335-28885413 | Common:2; Rare:61 | ||||
chr21:29019302-29019407 | Common:5; Rare:44 | ||||
chr21:29024534-29024776 | Common:2; Rare:104 | ||||
chr21:29024876-29025025 | Rare:29 | ||||
chr21:29073571-29073856 | Common:2; Rare:87 | ||||
chr21:29298638-29298953 | Common:3; Rare:126 | ||||
chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
chr21:32279017-32279191 | Common:3; Rare:78 | ||||
chr21:32392873-32393187 | Common:3; Rare:129 | ||||
chr21:32411634-32411815 | Rare:43 | ||||
chr21:32412337-32412730 | Common:2; Rare:85 | ||||
chr21:32612551-32612895 | Rare:85 | ||||
chr21:32727889-32728129 | Rare:118; Clinvar:2 | ||||
chr21:32771702-32772241 | Common:14; Rare:229 | ||||
chr21:33266262-33266473 | Rare:68; Clinvar:3 |